<p><strong>QA &ndash; Assistant Engineer</strong></p><p>Bio-pharmaceutical MNC in Tuas</p><p>We are looking for a Quality Assurance (QA) assistant to review GMP documents for manufacturing to ensure product quality.</p><p><strong>Job scope and responsibilities:</strong></p><ul><li>Document control and change control process for processes (e.g., upstream, downstream).</li><li>Review specifications, and qualification documents.</li><li>Liaise with process team (e.g. engineer) to identify end user requirements.</li><li>Support department in documentation related to QA, qualification/validation.</li><li>Any other duties as assigned by Quality Manager.</li><li>6 months contract (extension subjected to performance).</li></ul><p><strong>Requirements:</strong></p><ul><li>Familiar in validation terms, such as IQ, OQ, PQ and able to read P&amp;ID.</li><li>1-2 years of QA/Validation experience in biotech or pharmaceutical manufacturing.</li><li>Microsoft Words (Advance preferable) and Microsoft Excel</li><li>English - fluent in speaking and writing</li><li>BS degree in Science or Engineering or a related subject.</li></ul>